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Structure of 170838-83-2
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1-Boc-3-benzyl-3-piperidinecarboxylic acid features a protected piperidine scaffold with a benzylated nitrogen and a Boc-regulated carboxylic acid, enabling direct incorporation into complex alkaloid frameworks. The sterically shielded tertiary amine and bench-stable Boc group streamline synthetic workflows in medicinal chemistry, supporting efficient coupling and cyclization sequences under standard conditions.
1-Boc-3-benzyl-3-piperidinecarboxylic acid serves as a versatile building block for the synthesis of bioactive piperidine derivatives. The Boc group provides stable protection of the amine, enabling straightforward deprotection under mild acidic conditions. The benzyl substituent enhances solubility and facilitates downstream functionalization, while the carboxylic acid functionality supports efficient coupling reactions. This compound demonstrates excellent bench stability and compatibility with standard peptide and medicinal chemistry workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: